Found: 25
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Azithromycin-resistant Neisseria gonorrhoeae isolates in Guangzhou, China (2009-2013): coevolution with decreased susceptibilities to ceftriaxone and genetic characteristics.
- Published in:
- 2016
- By:
- Publication type:
- journal article
A recurrent R936X mutation of CYLD gene in a Chinese family with multiple familial trichoepithelioma.
- Published in:
- 2015
- By:
- Publication type:
- Letter to the Editor
Novel D323G mutation of DSG4 gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix.
- Published in:
- International Journal of Dermatology, 2015, v. 54, n. 10, p. 1163, doi. 10.1111/ijd.12889
- By:
- Publication type:
- Article
Novel Ala94 Thr mutation of keratin 14 in epidermolysis bullosa simplex.
- Published in:
- International Journal of Dermatology, 2014, v. 53, n. 10, p. e466, doi. 10.1111/ijd.12594
- By:
- Publication type:
- Article
Multiple familial trichoepithelioma: report of a Chinese family not associated with a mutation in the CYLD gene and CYLD protein expression in the trichoepithelioma tumor tissue.
- Published in:
- International Journal of Dermatology, 2014, v. 53, n. 4, p. e279, doi. 10.1111/ijd.12153
- By:
- Publication type:
- Article
Identification of a Novel Locus for Progressive Symmetric Erythrokeratodermia to a 19.02-cM Interval at 21q11.2–21q21.2.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Inversa Acne (Hidradenitis Suppurativa): A Case Report and Identification of the Locus at Chromosome 1p21.1–1q25.3.
- Published in:
- Journal of Investigative Dermatology, 2006, v. 126, n. 6, p. 1302, doi. 10.1038/sj.jid.5700272
- By:
- Publication type:
- Article
The Gene for a Rare Autosomal Dominant Form of Pompholyx Maps to Chromosome 18q22.1–18q22.3.
- Published in:
- Journal of Investigative Dermatology, 2006, v. 126, n. 2, p. 300, doi. 10.1038/sj.jid.5700103
- By:
- Publication type:
- Article
Identification of a Novel Locus for Marie Unna Hereditary Hypotrichosis to a 17.5 cM Interval at 1p21.1–1q21.3.
- Published in:
- Journal of Investigative Dermatology, 2005, v. 125, n. 4, p. 711, doi. 10.1111/j.0022-202X.2005.23874.x
- By:
- Publication type:
- Article
Identification of the Cylindromatosis Tumor-Suppressor Gene Responsible for Multiple Familial Trichoepithelioma.
- Published in:
- Journal of Investigative Dermatology, 2004, v. 122, n. 3, p. 658, doi. 10.1111/j.0022-202X.2004.22321.x
- By:
- Publication type:
- Article
A Gene for Freckles Maps to Chromosome 4q32–q34.
- Published in:
- Journal of Investigative Dermatology, 2004, v. 122, n. 2, p. 286, doi. 10.1046/j.0022-202X.2004.22244.x
- By:
- Publication type:
- Article
Fine Mapping of the Psoriasis Susceptibility Locus PSORS1 Supports HLA-C as the Susceptibility Gene in the Han Chinese Population.
- Published in:
- PLoS Genetics, 2008, v. 4, n. 3, p. 1, doi. 10.1371/journal.pgen.1000038
- By:
- Publication type:
- Article
The Epidemiology of Childhood Alopecia Areata in China: A Study of 226 Patients.
- Published in:
- 2006
- By:
- Publication type:
- Other
Association of HLA-DQA1 and DQB1 genes with vitiligo in Chinese Hans.
- Published in:
- International Journal of Dermatology, 2005, v. 44, n. 12, p. 1022, doi. 10.1111/j.1365-4632.2004.02389.x
- By:
- Publication type:
- Article
Comparison of Clinical Features of HLA-Cw*0602-Positive and -Negative Psoriasis Patients in a Han Chinese Population.
- Published in:
- Acta Dermato-Venereologica, 2007, v. 87, n. 4, p. 335, doi. 10.2340/00015555-0253
- By:
- Publication type:
- Article
Effect of repetitive transcranial magnetic stimulation-assisted training on lower limb motor function in children with hemiplegic cerebral palsy.
- Published in:
- BMC Pediatrics, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12887-024-04605-5
- By:
- Publication type:
- Article
Evidence for a Novel Psoriasis Susceptibility Locus at 9q33–9q34 in Chinese Hans.
- Published in:
- Journal of Investigative Dermatology, 2007, v. 127, n. 5, p. 1140, doi. 10.1038/sj.jid.5700671
- By:
- Publication type:
- Article
Complement C4 induces regulatory T cells differentiation through dendritic cell in systemic lupus erythematosus.
- Published in:
- Cell & Bioscience, 2015, v. 5, p. 1, doi. 10.1186/s13578-015-0052-8
- By:
- Publication type:
- Article
Intelligent collision avoidance based on two-dimensional risk model.
- Published in:
- Journal of Algorithms & Computational Technology, 2016, v. 10, n. 3, p. 131, doi. 10.1177/1748301816640251
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- Publication type:
- Article
Splicing mutation in MVK is a cause of porokeratosis of Mibelli.
- Published in:
- Archives of Dermatological Research, 2014, v. 306, n. 8, p. 749, doi. 10.1007/s00403-014-1465-7
- By:
- Publication type:
- Article
Genetic diagnosis in a Chinese Hailey–Hailey disease pedigree with novel ATP2C1 gene mutation.
- Published in:
- Archives of Dermatological Research, 2008, v. 300, n. 4, p. 203, doi. 10.1007/s00403-008-0834-5
- By:
- Publication type:
- Article
Five mutations of ATP2A2 gene in Chinese patients with Darier’s disease and a literature review of 86 cases reported in China.
- Published in:
- Archives of Dermatological Research, 2006, v. 298, n. 2, p. 58, doi. 10.1007/s00403-006-0658-0
- By:
- Publication type:
- Article
Association of HLA-DQA1 and DQB1 alleles with alolpecia areata in Chinese Hans.
- Published in:
- Archives of Dermatological Research, 2005, v. 297, n. 5, p. 201, doi. 10.1007/s00403-005-0608-2
- By:
- Publication type:
- Article
SHARPIN regulates cell proliferation of cutaneous basal cell carcinoma via inactivation of the transcriptional factors GLI2 and c-JUN.
- Published in:
- Molecular Medicine Reports, 2020, v. 21, n. 4, p. 1799, doi. 10.3892/mmr.2020.10981
- By:
- Publication type:
- Article
Mutation and expression of ABCA12 in keratosis pilaris and nevus comedonicus.
- Published in:
- Molecular Medicine Reports, 2018, v. 18, n. 3, p. 3153, doi. 10.3892/mmr.2018.9342
- By:
- Publication type:
- Article